Prenatal Maternal Hyperoxygenation Testing and Implications for Critical Care Delivery Planning among Fetuses with Congenital Heart Disease: Early Experience

被引:22
作者
Schidlow, David N. [1 ,2 ]
Donofrio, Mary T. [1 ,2 ]
机构
[1] Childrens Natl Hlth Syst, Childrens Natl Heart Inst, Washington, DC USA
[2] George Washington Univ, Sch Med & Hlth Sci, Dept Pediat Cardiol, Washington, DC 20052 USA
关键词
maternal hyperoxygenation; congenital heart disease; delivery planning; perinatal care; GREAT-ARTERIES; D-TRANSPOSITION; DIAGNOSIS; PREDICTION; REACTIVITY; FEATURES;
D O I
10.1055/s-0037-1603991
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background Maternal hyperoxygenation (MH) during fetal ultrasound can characterize fetal pulmonary vasoreactivity (PVr) and its associations with postnatal physiology. Objective We explored MH testing to facilitate perinatal risk stratification for fetuses with congenital heart disease (CHD). Methods MH was performed in 12 fetuses: 2 with Ebstein anomaly, 2 with total anomalous pulmonary venous connection (TAPVC), 4 with hypoplastic left heart syndrome (HLHS) with (a) restrictive atrial septum (RAS) or (b) intact atrial septum (IAS) with decompressing vertical vein (VV), and 4 with D-loop transposition of the great arteries (TGA). PVr and physiologic and anatomic changes with MH and outcomes were recorded. Results Among Ebstein fetuses, pulmonary blood flow with MH mirrored postnatal findings. Among TAPVC fetuses, MH VV gradients correlated with postnatal gradients. One HLHS/IAS/VV fetus had no PVr and decreased pulmonary vein forward to reverse velocity time integral ratio with MH. Shortly after delivery, the infant experienced severe low cardiac output and required urgent atrial septoplasty. The remaining HLHS fetuses had PVr and underwent routine Stage 1 Norwood. Among TGA fetuses, septum primum position, foramen ovale flow, and the presence or absence of PVr with MH reflected postnatal findings. Conclusion MH may help identify fetuses with CHD at risk for perinatal compromise. Additional study may yield insights into fetal PVr and elucidate predictors of perinatal outcomes.
引用
收藏
页码:16 / 23
页数:8
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